Washington Homeopathic Products recalls Z-1050 Formula Hepatodetox (1000ml) due to out-of-specification test results from HPTLC analysis. This product is for manufacturing use only and not intended for human consumption.
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Washington Homeopathic Products is recalling Z-1050 Formula Hepatodetox (1000ml) because lab tests showed it didn't meet quality standards. This product is only for manufacturing use and not meant for human consumption.
The product failed quality tests based on HPTLC analysis, meaning it doesn't meet the required specifications. However, since it's intended for manufacturing use only and not for human consumption, the risk to end users is minimal.
This recall affects manufacturers or facilities that use the product for production purposes. Consumers who purchased it for personal use are not affected since it's labeled for manufacturing only.
Check for the product name 'Z-1050 Formula Hepatodetox' with 1000ml capacity. It was manufactured by Washington Homeopathic Products, Inc. and sold with lot numbers 26071 or 28180, expiring August 17, 2026.
Look for the product name 'Z-1050 Formula Hepatodetox' and lot numbers 26071 or 28180.
No, this product is labeled for manufacturing use only and not intended for human consumption.
The product failed quality tests based on HPTLC analysis, indicating it does not meet the required specifications.
Since it's for manufacturing use only, consumers who purchased it for personal use are not affected. Manufacturers should follow their internal procedures for handling recalled materials.
We’ve drafted a message you can send Washington Homeopathic Products to request your refund or repair — edit it as you like.
Subject: Recall D-0883-2021 — Washington Homeopathic Products Washington Homeopathic Products Hello, I own a Washington Homeopathic Products that is covered by recall D-0883-2021 from Washington Homeopathic Products. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
